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Gender-affirming Hormone Therapy and Changes in Kidney Function in Adults: A Retrospective Population-based Study
Silvia J Leon1, Thomas W Ferguson1,2, Reid Whitlock1
1Chronic Disease Innovation Centre, Seven Oaks General Hospital, Winnipeg, Manitoba, Canada.
Gender-affirming hormone therapy (GAHT) may increase serum creatinine in transgender women. This study found no increased risk of kidney disease or hypertension with GAHT in transgender and gender diverse adults.
Area of Science:
- Endocrinology
- Nephrology
- Public Health
Background:
- Gender-affirming hormone therapy (GAHT) impacts body composition, but its effects on kidney function remain unclear.
- Understanding GAHT's renal impact is crucial for transgender and gender diverse (TGD) individuals' health.
Purpose of the Study:
- To investigate the association between GAHT and kidney function in TGD adults.
- To evaluate changes in serum creatinine, urine albumin-to-creatinine ratio, and risks of acute kidney injury, chronic kidney disease, and hypertension.
Main Methods:
- Retrospective observational cohort study using health administrative data from Manitoba, Canada (2007-2018).
- Compared TGD adults receiving GAHT versus those not, stratified by sex assigned at birth (AFAB and AMAB).
- Utilized multivariable regression and Cox proportional hazards models to assess outcomes up to 2 years post-prescription.
Main Results:
- In individuals assigned female at birth (AFAB) receiving GAHT, serum creatinine levels showed a statistically significant increase at 18 and 21 months compared to those without GAHT.
- No significant differences in creatinine changes were observed in individuals assigned male at birth (AMAB) receiving GAHT.
- Initiating GAHT was not associated with increased risks of incident chronic kidney disease or hypertension in either AFAB or AMAB individuals.
Conclusions:
- GAHT is associated with elevated serum creatinine levels in AFAB individuals.
- Further research is necessary to fully elucidate the long-term effects of GAHT on kidney function in TGD populations.
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